Method of curing organic polymers and copolymers

ABSTRACT

A curable composition is disclosed which comprises a hydroxylated organopolysiloxane fluid and an organic polymer having one or more silyl groups connected thereto. Each silyl group contains one or more groups capable of reacting with the hydroxyl groups of the organopolysiloxane.

United States Patent [1 1 Chadha Mar. 11, 1975 METHOD OF CURING ORGANIC POLYMERS AND COPOLYMERS [75] Inventor: Rajendra Nath Chadha,

Farmingdale, NY.

[73] Assignee: Stauffer Chemical Company, Adrian, Mich.

[22] Filed: Sept. 4, 1973 [21] Appl. No.: 394,215

Related US. Application Data [60] Division of Ser. No. l54,594, June 18, 1971, Pat. No. 3,776,977, which is a continuation-in-part of Ser. No. 37,409, May [1, 1970, abandoned.

[52] US. Cl. 260/825, 260/18 S, 260/46.5 G, 260/80 PS, 260/827 [51] Int. Cl. C08g 47/10 [58] Field of Search... 260/827, 80 PS. 825, 46.5 G

[56] References Cited UNITED STATES PATENTS 3,655,598 4/[972 Antonen et al 260/[8 S 3,655,633 v4/[972 Saam 260/465 G Primary Examiner-Melvyn l. Marquis [57] ABSTRACT 9 Claims, N0 Drawings METHOD OF CURING ORGANIC POLYMERS AND COPOLYMERS This is a division of application Ser. No. 154,594, filed June 18, I971, now US. Pat. No. 3,776,977 which is a continuation-in-part of Ser. No. 37,409, filed May 1 l, 1970 now abandoned.

This invention relates to a novel method for effecting the curing or vulcanization of organic polymers and copolymers. More particularly, the invention is con cerned with a method which is adapted to achieve the curing without the aid of extraneous heat or pressure i.e. under ambient conditions.

It is well known, that certain materials having a liquid, gum, gel or paste-like character may be cured by various means to achieve highly useful products. Thus natural rubber, for instance, is cured or vulcanized by treatment with sulfur and other chemicals at elevated temperatures, the rubber being thereby converted from a gummy mass to the tack-free elastomer well known to everyone. Many other organic polymers including both those classified as elastomers and those classified as plastics are cured similarly.

The requirement of elevated temperatures in these curing processes as practiced on an industrial scale represents a vast expenditure. This energy requirement accounts for a substantial portion of the cost of the elastomer or plastic. In addition, the requirement of extraneous heat negates against the use of, such plastics and elastomers in those cases where the curing must take place in situ in the presence of materials unadapted to withstand elevated temperatures.

As should be apparent from the foregoing, the invention has for its principal object the provision of a process for bringing about the curing of organic materials, particularly organic polymers and copolymers, at commonly experienced temperatures.

In accordance therewith, the stated object is accomplished through the incorporation in the organic material of one or more silyl groups, each of which contains one or more reactive groups, and a hydroxylated organopolysiloxane fluid.

The silyl groups may be represented by the formula in which R is a hydrocarbon radical or a halogenated hydrocarbon radical, X is a reactive radical, and z is a number from 1 to 3. The reactive radicals are capable of reacting with the hydroxyl groups of the organopolysiloxane to form small molecules of the formula HX, and a linkage of the type Si-O-Si, whereby the organic polymer becomes bonded to the organopolysiloxane.

Radicals represented by X, above include hydrogen, hydroxyl, alkoxy, aryloxy, halogen, acyloxy, phosphato, amino, amido, aminooxy and oximo. Of those that react spontaneously, the preferred radicals are acyloxy, e.g., acetoxy and propionoxy; amino, e.g., butylamino, cyclohexylamino, dimethylamino, and morpholino; oximo, e.g., acetoximo; and aminooxy, c.g., diethylaminooxy. Reactive radicals that require a catalyst are preferably hydrogen or an alkoxy radical, e.g., methoxy, ethoxy, propoxy, isopropoxy, and 2- methoxyethoxy.

The reactive radicals may react spontaneously with the hydroxyl groups, in which case, curing takes place rachlorosilane,

rapidly at room temperature. Alternatively. a catalyst may be required, in which case the composition is stable for long periods, and curing is effected only after the catalyst is added.

It is not necessary, that a large proportion of silyl groups be present. For minimum curing the total number of reactive groups should be at least three per molecule. This can be achieved by one silyl group of the type-SiX two of the type I? -Si)1 or three of the type Somewhat more than the minimum is generally preferred, depending on the degree of cross linking required. The total amount of silicon in the organic polymer may thus range from as little as l percentor less to as high as 20 percent, when a highly crosslinked product is desired. 7

The silyl group, may be incorporated by means of a silane in which the valence bond of the silicon shown as unsatisfied may be satisfied by hydrocarbon radicals,

such as, alkyl, aryl, alkaryl, aryalkyl, and cycloalkyl radicals. Alternatively, such unsatisfied valence bond may provide a link to an unsaturated hydrocarbon group, to an oxygen atom of an organopolysiloxane chain or ring or to another silicon atom, as in disilanes, trisilanes, etc. In these polysilanes, a plurality of the silicon atoms may have OH radicals or OI-I-convertible radicals attached thereto.

Among the many silyl compounds having application to the invention may be mentioned: trichlorosilane, tetmethyltrichlorosilane, methyldichlorosilane, 3-methylbutadienylmethyldimethoxysilane, dichlorodiethoxysilane, dibromodipropoxysilane,

vinyltriacetoxysilane, dichlorodipropionoxysilane, methyltrimethoxysilane, vinyltriethoxysilane, allyltrimethoxysilane, phenyltriacetoxysilane, methacrylatopropylsilane, butadienyltriacetoxysilane, butadienyltriethoxysilane, isopropyltriacetoxysilane, phenyltriacetoxysilane, propyltripropionoxysilane, ethyltriacetoxysilane, cyclohexyltripropoxysilane,

heptyltriisopropionoxysilane, silanediols and disiloxanediols e.g., dimethylsilanediol, diphenylsilanediol, tetramethyldisiloxanediol, etc.

The method herein is virtually unlimited as to the organic polymer or copolymer to which it is applied. However, as a matter of providing examples, polymers and copolymers based on the following organic monomers may be mentioned: unsaturated aliphatic hydrocarbons, such as ethylene, propylene, butylene, isoprene, butadiene; halogenated aliphatic hydrocarbons, such as vinyl chloride, vinylidene chloride, chlorobutadienes, alpha-methyl styrene, methyl acrylate, styrene, 2,5-dichlorostyrene, methacrylonitrile and methyl methacrylate.

Hydrocarbon-substituted homologues of any of the foregoing monomers, of course, are also applicable. Similarly, the many vinyl and diene monomers having a hydrocarbon backbone find utility in the practice of the invention.

The introduction of the functional silyl group or groups into the selected organo-polymer may be effected incident to the prepartion of the polymer or the polymer may be pre-prepared and the silyl group or groups subsequently introduced thereinto. Of the vari- 5 phthalic anhydride, malelc anhydride, and acid chloous specific ways whereby the silylization may be rides such as succinyl chloride, dodecanedioyl chloachieved, the following may be cited for illustration: ride, phthaloyl chloride and the like.

I. An unsaturated silane may be copolymerized with Examples of suitably hydroxyl terminated hydrocarvinyl-type organic monomers by known means. bons which may be reacted with the epoxyalkylsilanes Suitable unsaturated silanes adapted for this purare ethylene glycol, l,4-butylene glycol, 1.6- pose include vinyltrialkoxysilane, methylvinylhexamethylene glycol and the like. dialkoxysilane, vinyltriacetoxysilane, allylsilanes, The reaction between the organic polymer and the butadienylsilanes, isoprenylsilanes and silanes in silyl radical will proceed over a wide temperature which the double bond is as remote from the silicon rang ie, a a temper ure of from ab to ut atom a in meth r l t lgil 200C. and more preferably from about 40 to about 150C. ii Although the organopolysiloxanes are normally linclifcficl H ear polysiloxane fluids having terminal hydroxyl 6 T groups, a low degree of branching is permissible and a i small number of pendant hydroxyl groups may be presi Si(OC-CH i m ent. In any case, the total number of hydroxyl groups J should not exceed four per molecule. Two hydroxyl 2. A preformed organic polymer may be added to or r ups per molecule is the preferred number.

condensed with silanes by means of suitable func- The organic groups of the organopolysiloxane may tional groups. Examples include the following: be any monovalent hydrocarbon, halogenated monovaa. Addition of epoxyalkylsilanes to reactive groups lent hydrocarbon or cyanoalkyl groups. Examples of in the organic polymer: suitable alkyl groups are methyl, ethyl, propyl, and buo ecu Cll-Cll -0-(Cli -$i(OEt) no on 9 on on I l (EtO S1 CH2) 0C3 CllCh -0 --OC1l Cll3ll 0( CH2 Si out 3 b. Addition of hydroxyalkylsilanes to cyclic anhytyl; alkenyl groups such as vinyl and allyl, aryl groups dride groups in the organic polymers: Such as phenyl and tolyl; halogenated alkyl and aryl groups such as trifluoropropyl, chlorophenyl, and di- 0(6), six chlorophenyl and cyanoalkyl groups such as cyanopro- 2 l I 2 3 3 40 pyl and the like. Methyl and phenyl groups are highly a i suitable. In general, at least 50 percent of the groups 0 i should be methyl.

' Generally speaking, a satisfactory degree of cure is "C obtained by the reaction of the silylized organic poly- COOH Lumen six mer and the hydroxylated organopolysiloxane. If fur- 3 3 n ther cure is desired, it may be achieved by allowing unreacted X groups to react with atmospheric moisture. conlensamn f hydroxyalkylsllanes wlth acid In this reaction, two molecules of I-IX are formed and chloride groups m the Orgamc polymer: a new Si-O-Si crosslink is formed. For this reaction, it 2MP" six Cleo Cool g ;{l is necessary that the total number ofX groups in the or- 2 3 3 ganic polymer exceed the total number of OH groups in the ol siloxane. In an case, the rimar crosslink- X3Sl CH2)3 0C0 COO(CH2)3S1X3 ing tak es i alace by reactio n with the polysili axane. 3 A unsaturated il may b reacted i h an In the practice of the invention it is preferred to emganic polymer in the presence of free radicals: P y y SO much of the l Compound as is required Pu n cu Cli-S1(0Lt) gcn -cn -n PH any polymer susceptible to grafting e.g., to achieve the desired degree of chain-lengthening andpolyethylene, polyvinyl chloride, polyvinyl acetate, /or cross-linking, this being set by the properties repolypropylene, polymethyl methacrylate, polystyquired in the finished product. A highly cross-linked rene, etc. product may require as much as 20 percent elemental Examples of suitable silanes are epoxyalkyl silanes 5 silicon based on the weight of the hybrid polymeric masuch as 'y-glycidoxypropyltriethoxysilane, 'y-glycidoxypropyltripropoxysilane, 'y-glycidoxypropyltrimethoxysilane, 'y-glycidoxyhexyltributoxysilane, 4,5- epoxypentatriethoxysilane, 5,6-epoxyhexyltributoxysilane, etc.; hydroxyalkylsilanes such as hydroxyethyltrimethoxysilane, hydroxypropyltrimethoxysilane. hydroxyhexyltributoxysilane and the like.

Organic compounds which may be reacted with the hydroxyalkylsilanes are cyclic anhydrides such as.

terial. On the other hand, in some cases as little as 1 percent or less elemental silicon in the product polymer may answer to specifications.

Although the reaction between the silylized organic polymer and the hydroxylated organopolysiloxane may occur at room temperature, the reaction may be accelerated by heating the reactants to a temperature of from about 30 to about 150C., more preferably from about 30 to about 70C.

Certain of the reactions herein leading to the silylcontaining polymers require a catalyst while others proceed satisfactorily without the aid of a catalyst. In any case, the water required for the hydrolysis and cross-linking of the polymer is normally derived ambiently. The equation below is supplied to illustrate the hydrolysis and cross-linking. In the particular case an organotin catalyst is employed to promote the hydrolysis:

:SHOHJCH Further cross-linking, it will be understood, results from hydrolysis of the remaining acyloxy groups.

Other catalysts which may be employed are metal salts of carboxylic acids such as lead, tin, zirconium, iron, cadmium, titanium, calcium and manganese salts of carboxylic acids. It is preferred, that the carboxylic acid radical contain less than I4 carbon atoms and more preferably from about 2 to carbon atoms. Examples of suitable salts are metal naphthenates, propenates, butyrates, laurates, such as, dibutyltin dilaurate and the like. Other organometallic compounds are dibutyltin butoxy chloride, bis-(acetoxydibutyltin)oxide, benzylbutylphenyltin hydroxide, di-t-butylchlorotin hydroxide and the like.

The catalysts are effective in minimal amounts, e.g., from about 0.02 to about 2 percent, preferably from about 0.1 to about 1 percent, by weight based on the weight of the composition.

The composition herein described have many applications, such as, sealants, as insulation material for electrical components, gasket materials, and shock absorbers.

The invention is further illustrated by the following examples which are not to be taken as in any way limitative thereof.

EXAMPLE I To a dry nitrogen-purged, 3-neck, 500-ml., roundbottom flask equipped with a thermometer, stirrer, gas inlet and condenser were added 98 grams of styrene, 2 grams of 3-methylbutadienylmethyldimethoxysilane and 3 grams of lauroylperoxide. The whole was heated to 70C. and maintained at such temperature for approximately 2% hours. At this time, the viscosity had increased to a molasses consistency. Five grams of CBr, were added to terminate the reaction, whereafter the residual monomers were stripped at reduced pressure.

6 Result: 84 grams of a high-viscosity product-Si anal.:0.36%.

A portion of the product was dissolved in acetone and precipitated with methanol to remove the low molecular weight polymers. Result: A solid product-Si anal.:0.5l%.

The stripped product and hydroxylated organopolysiloxane fluid (2300 cp.) were mixed in 1:1 weight ratio, catalyzed with stannous octoate, and allowed to cure. Result: A white opaque rubbery product.

EXAMPLE 2 To a flask as described in Example 1 were added 98 grams of styrene, 2 grams of 3-methylbutadienylmethyldiacetoxysilane and 3 grams of azobisisobutyronitrile. The whole was heated to C. and maintained at such temperature for approximately 2% hours. This increased the viscosity of the mixture significantly. At this stage, 1 ml. of silicon tetrabromide was added to terminate the reaction. The residual monomers were then stripped at reduced pressure. Result: 76.5 grams of a yellow-tan, high-viscosity (Gardner Y-Z viscosity) product.

A portion of the product was cast on a glass plate and allowed to cure in air. Result: A fairly flexible, tough film.

A second portion of the product was mixed in 1:] weight ratio with hydroxylated organopolysiloxane fluid (2,600 cp.), cast on a glass plate and allowed to air-cure. Result: A white opaque rubber material.

EXAMPLE 3 Low molecular weight polyisoprene with living" ends was prepared using an initiator made up of the following materials:

Naphthalene l0 gm. Tetrahydrofuran (anhydrous) 35 gm. Sodium 3 gm. (excess) The initiator components were stirred under nitrogen at room temperature overnight, whereafter the resulting dark green solution was decanted from the excess sodium and stored under nitrogen.

The polymerization of the isoprene was carried out in dry nitrogen-flushed ampoules at 0C. In each case, 10 ml. of isoprene was added dropwise to 2 mol. of the initiator solution diluted with 28 ml. of the anhydrous THF. The resulting solutions became viscous and turned pink to red in color.

An increment of dichlorodiethoxysilane was added to the polymer solution, resulting in a viscosity increase and discharge of the pink color. The excess of silane was removed by vacuum distillation. When samples of this material were mixed with organopolysiloxane hydroxy fluid (2300 cp.) and stannous octoate a cured rubber of desirable properties resulted.

EXAMPLE 4 In this experiment the following materials in the quantities indicated were utilized:

Carboxy-terminated polybutadiene (MW. 5000) 100.0 gm. Glycidoxypropyltrimethoxysilane 9.4 gm. N,N-dimethylaniline 0.5 ml.

EXAMPLE To a nitrogen-purged, 3-neck, ZOOO-ml. flask equipped with a condenser, thermometer, mechanical agitator and a gas inlet were added 500 grams of 1,2- polybutadiene, 300 ml. of dry toluene and 2.0 ml. of a 0.4N solution of chloroplatinic acid in isopropyl alcohol. The temperature of the whole was increased to 40C. afterwhich 100 grams of methyldimethoxysilane were added dropwise. The temperature was then increased to 55C. and maintained thereat for 16 hours. The product was precipitated with methanol, separated and dried at 50C. under vacuum (25 in. Hg) for 24 hours. Result: Si anal.;3 .90% 91.2% theoretical yield.

A portion of the product was applied as follows:

100 parts (by weight) polymer 40 parts carbon black (continex F-3) parts 2800 cp. hydroxylated organopolysiloxane fluid 2 parts tin catalyst A sample specimen of the thoroughly mixed, filled product was pressed into a window mold and the sample allowed to cure at room temperature. A tough rubbery product resulted.

EXAMPLE 6 A polysiloxane was prepared from the following:

Styrene 104.00 gm. Vinyltriethoxysilane 10.50 gm. organopolysiloxane OH-Fluid (1300 cps.) 114.50 gm. Di-t-butylperoxide (catalyst) 0.11 gm.

The polymerization was carried out at 125C. under nitrogen in a 500-ml. flask equipped with a mechanical agitator. The reaction was stopped after 27 hours by vacuum distillation of unreacted monomers. The product was an opaque white fluid soluble in toluene. When a portion of this product was mixed with a catalytic amount of stannous octoate it cured to a strong resilient rubber.

The invention claimed is:

l. A curable composition comprising a hydroxylated organopolysiloxane fluid and a silylated organic polymer having one or more silyl groups of the formula connected thereto, wherein R is selected from the group consisting of hydrocarbon radicals and halogenated hydrocarbon radicals, X is a reactive group capable of condensing with the hydroxyl groups of the organopolysiloxane, and z is a number of from 1 to 3, said silylated organic polymer being derived from organic monomers containing a carbon-to-carbon double bond and contains at least 3 reactive X groups per molecule.

2. The composition of claim 1 wherein X represents an acyloxy radical.

3. The composition of claim 1 wherein X represents an alkoxy radical.

4. The composition of claim 1 wherein the silylated organic polymer contains from 1 to about 20 percent silicon.

5. The composition of claim 2 wherein said acyloxy radicals are acetoxy radicals.

6. The composition of claim 1 wherein z is equal to 3.

7. The cured composition of claim 6 wherein said composition is exposed to atmospheric moisture.

8. The curable composition of claim 1 wherein the silylated organic polymeric is obtained by copolymerizing a silane having a carbon-to-carbon double bond with the organic monomers of claim 1.

9. The composition of claim 1 wherein X is selected from the group consisting of hydrogen, hydroxyl, alkoxy, aryloxy, halogen, acyloxy, phosphato, amino,

amido, aminooxy, and oximo groups. 

1. A CURABLE COMPOSITION COMPRISING A HYDROXYLATED ORGANOPOLYSILOXANE FLUID AND A SILYLATED ORGANIC POLYMER HAVING ONE OR MORE SILYL GROUPS OF THE FORMULA
 1. A curable composition comprising a hydroxylated organopolysiloxane fluid and a silylated organic polymer having one or more silyl groups of the formula
 2. The composition of claim 1 wherein X represents an acyloxy radical.
 3. The composition of claim 1 wherein X represents an alkoxy radical.
 4. The composition of claim 1 wherein the silylated organic polymer contains from 1 to about 20 percent silicon.
 5. The composition of claim 2 wherein said acyloxy radicals are acetoxy radicals.
 6. The composition of claim 1 wherein z is equal to
 3. 7. The cured composition of claim 6 wherein said composition is exposed to atmospheric moisture.
 8. The curable composition of claim 1 wherein the silylated organic polymeric is obtained by copolymerizing a silane having a carbon-to-carbon double bond with the organic monomers of claim
 1. 